Enoxaparin Sodium (Amphastar Pharmaceuticals, Inc.)
Welcome to the PulseAid listing for the Enoxaparin Sodium drug offered from Amphastar Pharmaceuticals, Inc.. This Heparin, Low-Molecular-Weight [Chemical/Ingredient],Low Molecular Weight Heparin [EPC] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
LABELER NAME / MANUFACTURER: | Amphastar Pharmaceuticals, Inc. |
NON-PROPRIETARY NAME: | Enoxaparin sodium |
SUBSTANCE NAME: | ENOXAPARIN SODIUM |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Heparin, Low-Molecular-Weight [Chemical/Ingredient],Low Molecular Weight Heparin [EPC] |
ROUTE: | SUBCUTANEOUS |
DOSAGE FORM: | INJECTION |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2011-09-19 |
END MARKETING DATE: | 0000-00-00 |
Enoxaparin Sodium HUMAN PRESCRIPTION DRUG Details:
Item Description | Enoxaparin Sodium from Amphastar Pharmaceuticals, Inc. |
LABELER NAME: | Amphastar Pharmaceuticals, Inc. |
DEA SCHEDULE: |
|
ACTIVE STRENGTH: | 100(mg/mL) |
START MARKETING DATE: | 2011-09-19 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0548-5601_b3c1914d-5633-45a5-a1b1-952a5665ae58 |
PRODUCT NDC: | 0548-5601 |
APPLICATION NUMBER: | ANDA076684 |
Other ENOXAPARIN SODIUM Pharmaceutical Manufacturers / Labelers: